Literature DB >> 9004148

Does preconditioning act by glycogen depletion in the isolated rat heart?

L M King1, L H Opie.   

Abstract

Preconditioning hastens the time to onset of ischaemic contracture and increases peak contracture in an isolated perfused rat heart, but improves recovery of function. The preconditioning ischaemic episode is also known to deplete glycogen stores. We tested whether a depletion in glycogen is related to the protection conferred by preconditioning. The isolated Langendorff perfused rat heart, with a left ventricular balloon to record function, was perfused with either glucose 11 mM, acetate 5 mM, or glucose 11 mM + insulin to alter pre-ischaemic glycogen levels prior to 30 min total global ischaemia. In addition, hearts were preconditioned by an episode of 5 min ischaemia and 5 min reperfusion. Time to onset of contracture (TOC-min), peak contracture and recovery of developed pressure after 20 min reperfusion with glucose-containing perfusate (both expressed as percentage pre-ischaemic developed pressure) were measured (n = 9-10). Parallel groups of hearts were clamped at various times for assessment of tissue metabolites. Acetate pre-perfusion reduced glycogen levels compared to glucose hearts, from 16.27 +/- 0.44 to 10.77 +/- 0.96 mumol/g wet wt. TOC was reduced and peak contracture increased, with poor functional recovery. Glucose + insulin pre-perfusion increased glycogen (21.39 +/- 1.08 mumol/g wet wt) with opposite effects on contracture, but functional recovery was still poor. Preconditioning hastened the time to onset of contracture, which could be partially attributed to glycogen depletion. Preconditioning significantly improved functional recovery in glucose hearts, but had little or no effect in the other groups. Thus the protective effect on functional recovery could not be linked to glycogen depletion. Pre-ischaemic glycogen appeared to play a dual role. When low, preconditioning was ineffective, presumably because of lack of production of glycolytic ATP, and severe contracture. When pre-ischaemic glycogen was increased, preconditioning was also relatively ineffective, presumably because of excess accumulation of the metabolites of glycogenolysis.

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Year:  1996        PMID: 9004148     DOI: 10.1006/jmcc.1996.0224

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  9 in total

1.  Mechanisms whereby glucose deprivation triggers metabolic preconditioning in the isolated rat heart.

Authors:  M M Awan; S Makaula; S Forresti; M N Sack; L H Opie
Journal:  Mol Cell Biochem       Date:  2000-08       Impact factor: 3.396

Review 2.  Glucose and glycogen utilisation in myocardial ischemia--changes in metabolism and consequences for the myocyte.

Authors:  L M King; L H Opie
Journal:  Mol Cell Biochem       Date:  1998-03       Impact factor: 3.396

3.  Myocardial subcellular glycogen distribution and sarcoplasmic reticulum Ca2+ handling: effects of ischaemia, reperfusion and ischaemic preconditioning.

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Journal:  J Muscle Res Cell Motil       Date:  2019-10-19       Impact factor: 2.698

4.  Essential role of nitric oxide in acute ischemic preconditioning: S-nitros(yl)ation versus sGC/cGMP/PKG signaling?

Authors:  Junhui Sun; Angel M Aponte; Mark J Kohr; Guang Tong; Charles Steenbergen; Elizabeth Murphy
Journal:  Free Radic Biol Med       Date:  2012-09-16       Impact factor: 7.376

Review 5.  Mechanisms underlying acute protection from cardiac ischemia-reperfusion injury.

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Journal:  Physiol Rev       Date:  2008-04       Impact factor: 37.312

Review 6.  The role of succinate and ROS in reperfusion injury - A critical appraisal.

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Journal:  J Mol Cell Cardiol       Date:  2017-07-05       Impact factor: 5.000

7.  Extent of mitochondrial hexokinase II dissociation during ischemia correlates with mitochondrial cytochrome c release, reactive oxygen species production, and infarct size on reperfusion.

Authors:  Philippe Pasdois; Joanne Elizabeth Parker; Andrew Philip Halestrap
Journal:  J Am Heart Assoc       Date:  2012-12-31       Impact factor: 5.501

Review 8.  The role of hexokinase in cardioprotection - mechanism and potential for translation.

Authors:  Andrew P Halestrap; Gonçalo C Pereira; Philippe Pasdois
Journal:  Br J Pharmacol       Date:  2014-11-24       Impact factor: 8.739

9.  Cyclophilin D ablation is associated with increased end-ischemic mitochondrial hexokinase activity.

Authors:  Rianne Nederlof; Mark A M van den Elshout; Anneke Koeman; Laween Uthman; Iris Koning; Otto Eerbeek; Nina C Weber; Markus W Hollmann; Coert J Zuurbier
Journal:  Sci Rep       Date:  2017-10-06       Impact factor: 4.379

  9 in total

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